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yoni יוני (@Primary_Immune)

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5 0 0 0 OA A Case of STAT1 Mutations in Chronic Mucocutaneous Candidiasis Diagnosed in an Adult

RT @murphbn: A Case of STAT1 Mutations in Chronic Mucocutaneous Candidiasis Diagnosed in an Adult https://t.co/NcHkC05009 #primaryimmunode…

8 0 0 0 OA Two Cases of Familial Mediterranean Fever Involving MEFV Variants: The Importance of Differentiating the Diagnosis from COVID-19

"FMV" is a rare

12 0 0 0 OA Successful Elimination of SARS-CoV-2 Following Vaccination with BNT162b2 after Prolonged Viral Infection in an Immunocompromised Lymphoma Patient

RT @Primary_Immune: Quite a remarkable

12 0 0 0 OA Successful Elimination of SARS-CoV-2 Following Vaccination with BNT162b2 after Prolonged Viral Infection in an Immunocompromised Lymphoma Patient

Quite a remarkable

7 0 0 0 COVID-19を契機に溶血発作を呈した非典型溶血性尿毒症症候群

Elated to see this

8 0 0 0 OA Combined Mutation of the GATA2 Gene and STAT5B Gene in a Patient with Hypogammaglobulinemia and Autoimmunity

Conventional wisdom would say that: "immunodeficiency and autoimmunity can't co-exist"

6 0 0 0 Aldehyde degradation deficiency(ADD)症候群 —アルデヒド代謝酵素欠損によるファンコニ貧血症類似の新たな遺伝性骨髄不全症候群の発見—

I have institutional-access to sci/med journals but not this one. Can any #medtwitter person access this pdf? Would appreciate greatly. Will be off Twitter for next 24 hours. https://t.co/fcr1rx0FJj #snrtg #openscience #scicomm #hematology #immunology #PrimaryImmunodeficiency https://t.co/8A9SFpvl1g

26 0 0 0 OA A novel frame shift mutation in STIM1 gene causing primary immunodeficiency

RT @Primary_Immune: Every novel #PrimaryImmunodeficiency genomic discovery is exceptional and heartening ...when it changes the life of a…

26 0 0 0 OA A novel frame shift mutation in STIM1 gene causing primary immunodeficiency

Every novel #PrimaryImmunodeficiency genomic discovery is exceptional and heartening ...when it changes the life of a young child, it's all the more so https://t.co/U3ey6hT9XJ #100DaysofCode #bigdata #iot #itrtg #openscience #technology #genomics #immunology #raredisease https://t.co/AX2WzTIy1a

お気に入り一覧（最新100件）

5 0 0 0 OA A Case of STAT1 Mutations in Chronic Mucocutaneous Candidiasis Diagnosed in an Adult

A Case of STAT1 Mutations in Chronic Mucocutaneous Candidiasis Diagnosed in an Adult https://t.co/NcHkC05009 #primaryimmunodeficiency

8 0 0 0 OA Two Cases of Familial Mediterranean Fever Involving MEFV Variants: The Importance of Differentiating the Diagnosis from COVID-19

"FMV" is a rare

12 0 0 0 OA Successful Elimination of SARS-CoV-2 Following Vaccination with BNT162b2 after Prolonged Viral Infection in an Immunocompromised Lymphoma Patient

Quite a remarkable

yoni יוני (@Primary_Immune)

投稿一覧（最新100件）

5 0 0 0 OA A Case of STAT1 Mutations in Chronic Mucocutaneous Candidiasis Diagnosed in an Adult

8 0 0 0 OA Two Cases of Familial Mediterranean Fever Involving MEFV Variants: The Importance of Differentiating the Diagnosis from COVID-19

12 0 0 0 OA Successful Elimination of SARS-CoV-2 Following Vaccination with BNT162b2 after Prolonged Viral Infection in an Immunocompromised Lymphoma Patient

12 0 0 0 OA Successful Elimination of SARS-CoV-2 Following Vaccination with BNT162b2 after Prolonged Viral Infection in an Immunocompromised Lymphoma Patient

7 0 0 0 COVID-19を契機に溶血発作を呈した非典型溶血性尿毒症症候群

8 0 0 0 OA Combined Mutation of the GATA2 Gene and STAT5B Gene in a Patient with Hypogammaglobulinemia and Autoimmunity

6 0 0 0 Aldehyde degradation deficiency(ADD)症候群 —アルデヒド代謝酵素欠損によるファンコニ貧血症類似の新たな遺伝性骨髄不全症候群の発見—

26 0 0 0 OA A novel frame shift mutation in STIM1 gene causing primary immunodeficiency

26 0 0 0 OA A novel frame shift mutation in STIM1 gene causing primary immunodeficiency

お気に入り一覧（最新100件）

5 0 0 0 OA A Case of STAT1 Mutations in Chronic Mucocutaneous Candidiasis Diagnosed in an Adult

8 0 0 0 OA Two Cases of Familial Mediterranean Fever Involving MEFV Variants: The Importance of Differentiating the Diagnosis from COVID-19

12 0 0 0 OA Successful Elimination of SARS-CoV-2 Following Vaccination with BNT162b2 after Prolonged Viral Infection in an Immunocompromised Lymphoma Patient

7 0 0 0 COVID-19を契機に溶血発作を呈した非典型溶血性尿毒症症候群

8 0 0 0 OA Combined Mutation of the GATA2 Gene and STAT5B Gene in a Patient with Hypogammaglobulinemia and Autoimmunity

6 0 0 0 Aldehyde degradation deficiency(ADD)症候群 —アルデヒド代謝酵素欠損によるファンコニ貧血症類似の新たな遺伝性骨髄不全症候群の発見—

26 0 0 0 OA A novel frame shift mutation in STIM1 gene causing primary immunodeficiency

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